Evidence map›Paper›PMID 40706783›Full record

ArticleActa biomaterialia2025

Equine influenza antigen-based particle vaccine protects mice against homologous and heterosubtypic viral challenges.

A C Siddoway, A Van Zanten, D Verhoeven, M J Wannemuehler, S K Mallapragada, B Narasimhan

Abstract read
In one paragraph

Article in Acta biomaterialia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

A C SiddowayDepartment of Chemical & Biological Engineering, Iowa State University, Ames, IA 50011, USA; Nanovaccine Institute, Iowa State University, Ames, IA 50011, USA.
A Van ZantenDepartment of Chemical & Biological Engineering, Iowa State University, Ames, IA 50011, USA.
D VerhoevenDepartment of Veterinary Microbiology & Preventive Medicine, Iowa State University, Ames, IA 50011, USA; Nanovaccine Institute, Iowa State University, Ames, IA 50011, USA.
M J WannemuehlerDepartment of Veterinary Microbiology & Preventive Medicine, Iowa State University, Ames, IA 50011, USA; Nanovaccine Institute, Iowa State University, Ames, IA 50011, USA.
S K MallapragadaDepartment of Chemical & Biological Engineering, Iowa State University, Ames, IA 50011, USA; Nanovaccine Institute, Iowa State University, Ames, IA 50011, USA.
B NarasimhanDepartment of Chemical & Biological Engineering, Iowa State University, Ames, IA 50011, USA; Nanovaccine Institute, Iowa State University, Ames, IA 50011, USA. Electronic address: nbalaji@iastate.edu.

Funding

Universal room temperature stable influenza nanovaccineR01AI141196 · NIAID · IOWA STATE UNIVERSITY · PI NARASIMHAN, BALAJI · 2019 to 2023
$5.6M
Combination nanovaccine-based immunization against influenza virus in the aged: immunity and protectionR01AI154458 · NIAID · IOWA STATE UNIVERSITY · PI KOHUT, MARIAN L, NARASIMHAN, BALAJI · 2021 to 2025
$3.5M
NIAID NIH HHS R01 AI141196NIAID NIH HHS R01 AI154458
6 · The paper itself

Abstract

Influenza virus is a common source of respiratory illness and poses a major public health burden globally. Significant efforts have been dedicated towards developing and deploying effective vaccines. However, since being licensed in 1945, influenza vaccines have made limited progress and still suffer from several limitations, including suboptimal efficacy against variants. In this work, we report on two influenza A polyanhydride particle- and pentablock copolymer-based vaccine formulations intended for intranasal or subcutaneous administration. These nanovaccines are based on a newly discovered equine influenza A H3N8 hemagglutinin antigen (A/equine/1/KY/91), A/HK/1/68 nucleoprotein antigen, and a small molecule adjuvant. When these nanovaccines were administered to naïve mice, both formulations induced robust humoral and cellular immune responses that were protective against lethal challenges with influenza A/HK/1/68 (H3N2) or A/PR/8/34 (H1N1). This protection was characterized by reduced viral load, reduced airway disruption, and preservation of weight post-infection. Further studies with immunization and challenge of CD8

Indexed as

Antigens, ViralInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza A Virus, H3N8 SubtypeInfluenza VaccinesOrthomyxoviridae InfectionsAnimalsFemaleHorsesMiceMice, Inbred BALB CAntigens, ViralInfluenza VaccinesEquine antigenInfluenzaParticlesPolyanhydridesProtective immunityVaccine

Identifiers

PMID40706783
PMCPMC12798653

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.